Canonical Allele Identifier: PA2828474889
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 194555

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358176.1:p.Arg853Gln
CA210022
NM_001371247.1:c.2558G>A